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581060-27-7

581060-27-7 Structure

581060-27-7 Structure
IdentificationBack Directory
[Name]

tert-butyl 4-(mercaptomethyl)piperidine-1-carboxylate
[CAS]

581060-27-7
[Synonyms]

1-Boc-4-(Mercaptomethyl)
1-Boc-4-(MercaptoMethyl)piperidine
tert-butyl 4-(sulfanylmethyl)piperidine-1-carboxylate
tert-butyl 4-(mercaptomethyl)piperidine-1-carboxylate
4-Mercaptomethyl-piperidine-1-carboxylic acid tert-butyl ester
4-(Mercaptomethyl)-1-piperidinecarboxylic acid tert-butyl ester
1-Piperidinecarboxylic acid, 4-(mercaptomethyl)-, 1,1-dimethylethyl ester
[Molecular Formula]

C11H21NO2S
[MOL File]

581060-27-7.mol
[Molecular Weight]

231.35
Chemical PropertiesBack Directory
[Boiling point ]

316.9±15.0 °C(Predicted)
[density ]

1.052
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[pka]

10.23±0.10(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C11H21NO2S/c1-11(2,3)14-10(13)12-6-4-9(8-15)5-7-12/h9,15H,4-8H2,1-3H3
[InChIKey]

VEPAXJUGIFPJNK-UHFFFAOYSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCC(CS)CC1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H412
[Precautionary statements ]

P273
Spectrum DetailBack Directory
[Spectrum Detail]

tert-butyl 4-(mercaptomethyl)piperidine-1-carboxylate(581060-27-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Piperidinecarboxylic acid, 4-[[(aminoiminomethyl)thio]methyl]-, 1,1-dimethylethyl ester

895126-44-0

tert-butyl 4-(mercaptomethyl)piperidine-1-carboxylate

581060-27-7

A reaction was carried out with tert-butyl 4-((carbamoylimidothio)methyl)piperidine-1-carboxylate (1.2, 15 g, 1.00 eq., crude) as raw material with sodium hydroxide (2.2 g, 55.00 mmol, 1.00 eq.) in a mixture of methanol/water (1:2 v/v, 150 mL) under argon protection at 60 °C with stirring for 2 hours. After completion of the reaction, the reaction mixture was cooled to room temperature. The pH of the reaction solution was adjusted with 35% aqueous hydrochloric acid to 7. The reaction solution was extracted with ethyl acetate (3 x 50 mL) and the organic phases were combined. The organic phase was washed with saturated saline (2 x 50 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether=1:8 v/v) to give 5.6 g of yellow oily product in 44% yield. The structure of the product was confirmed by 1H-NMR (400 MHz, CDCl3): δ 4.13 (m, 2H), 2.69 (m, 2H), 2.46 (m, 2H), 1.82 (m, 2H), 1.50 (s, 9H), 1.32 (m, 1H), 1.18 (m, 2H) ppm.

[References]

[1] Patent: US2016/243100, 2016, A1. Location in patent: Paragraph 0078
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